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Edward B Holson

Showing results (1-10 of 38) with videos related to

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Organic Letters|October 12, 2002
Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketalsEdward B Holson, William R Roush
Organic Letters|October 12, 2002
Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reactionEdward B Holson, William R Roush
Nature Biotechnology|March 11, 2011
Chemoproteomics quantifies complexityEdward B Holson, Stuart L Schreiber
Organic Letters|May 9, 2003
Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanesJung-Nyoung Heo, Edward B Holson, William R Roush
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 9, 2013
Small molecule inhibitors of zinc-dependent histone deacetylasesFlorence F Wagner, Michel Weїwer, Michael C Lewis, et al.
Future Medicinal Chemistry|September 13, 2013
Therapeutic potential of isoform selective HDAC inhibitors for the treatment of schizophreniaMichel Weïwer, Michael C Lewis, Florence F Wagner, et al.
ACS Chemical Biology|January 27, 2010
Characterization of plant-derived saponin natural products against Candida albicansJeffrey J Coleman, Ikechukwu Okoli, George P Tegos, et al.
The Journal of Biological Chemistry|September 2, 2017
Isoform-selective inhibitor of histone deacetylase 3 (HDAC3) limits pancreatic islet infiltration and protects female nonobese diabetic mice from diabetesErcument Dirice, Raymond W S Ng, Rachael Martinez, et al.
Chemistry & Biology|April 21, 2015
Hydroxamate-based histone deacetylase inhibitors can protect neurons from oxidative stress via a histone deacetylase-independent catalase-like mechanismDavid E Olson, Sama F Sleiman, Megan W Bourassa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 31, 2013
Signal-dependent repression of DUSP5 by class I HDACs controls nuclear ERK activity and cardiomyocyte hypertrophyBradley S Ferguson, Brooke C Harrison, Mark Y Jeong, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Organic Letters|October 12, 2002
Synthesis of the C(2)-C(13) fragment (the A-B spiroketal unit) of spongistatin 1 (altohyrtin A): use of a common intermediate for the synthesis of both spongistatin spiroketalsEdward B Holson, William R Roush
Organic Letters|October 12, 2002
Diastereoselective synthesis of the C(17)-C(28) fragment (the C-D spiroketal unit) of spongistatin 1 (altohyrtin A) via a kinetically controlled iodo-spiroketalization reactionEdward B Holson, William R Roush
Nature Biotechnology|March 11, 2011
Chemoproteomics quantifies complexityEdward B Holson, Stuart L Schreiber
Organic Letters|May 9, 2003
Common-intermediate strategy for synthesis of conduritols and inositols via beta-hydroxy cyclohexenylsilanesJung-Nyoung Heo, Edward B Holson, William R Roush
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 9, 2013
Small molecule inhibitors of zinc-dependent histone deacetylasesFlorence F Wagner, Michel Weїwer, Michael C Lewis, et al.
Future Medicinal Chemistry|September 13, 2013
Therapeutic potential of isoform selective HDAC inhibitors for the treatment of schizophreniaMichel Weïwer, Michael C Lewis, Florence F Wagner, et al.
ACS Chemical Biology|January 27, 2010
Characterization of plant-derived saponin natural products against Candida albicansJeffrey J Coleman, Ikechukwu Okoli, George P Tegos, et al.
The Journal of Biological Chemistry|September 2, 2017
Isoform-selective inhibitor of histone deacetylase 3 (HDAC3) limits pancreatic islet infiltration and protects female nonobese diabetic mice from diabetesErcument Dirice, Raymond W S Ng, Rachael Martinez, et al.
Chemistry & Biology|April 21, 2015
Hydroxamate-based histone deacetylase inhibitors can protect neurons from oxidative stress via a histone deacetylase-independent catalase-like mechanismDavid E Olson, Sama F Sleiman, Megan W Bourassa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 31, 2013
Signal-dependent repression of DUSP5 by class I HDACs controls nuclear ERK activity and cardiomyocyte hypertrophyBradley S Ferguson, Brooke C Harrison, Mark Y Jeong, et al.
Pageof 4